FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FLOSWITCH(R) HP

K Number: K913871 · Decision Nov 25, 1991
Classifications
1
FEI Numbers
213
Registration Numbers
214
Same Product Code
497
Applicant Total
430
Review Days
89

Basic Information

Device Name
FLOSWITCH(R) HP
K Number
K913871
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BOSTON SCIENTIFIC CORP.
Date Received
August 28, 1991
Decision Date
November 25, 1991
Product Code
DQO
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQO Catheter, Intravascular, Diagnostic

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